Donna M McDonald-McGinn (Donna McDonald-McGinn, D M McDonald-McGinn)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 43

Top Venues

Genes

Research square

Molecular psychiatry

Science (New York, N.Y.)

This page only lists publications with an associated author ORCID identifier.

Publications

Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, Terrence Blaine Crowley, Stephanie Asher, Amanda Back, Sarah M Baldino, Emma Bedoukian, Allison D Britt, Natalie Burrill, Cara Cacioppo, Dana Farengo Clark, Mary Egan Clark, Laura Conway, Laynie Dratch, Holly A Dubbs, Nicole M Engelhardt, Natalie Ginn, Christopher Gray, Tiff Hartman, Evan R Hathaway, Katherine L Helbig, Lily Hoffman-Andrews, Stefanie Kasperski, Beth A Keena, Kierstin N Keller, Katherine L Nathanson, Lauren Lulis, Laina Lusk, Daniel E McGinn, Rebecca Mueller, Rache A Paul, Lisa Pilchman, Jacquelyn Powers, Sarah E Raible, Sara Reichert, Alyssa L Ritter, Angela G Arnold, Sarah M Ruggiero, Erica Schindewolf, Katie Rose Sullivan, Shannon Terek, Bekah Wang, McKenzie Wells, Natalia Wisniewski, Renee Wright, Elisabeth McCarty Wood, Stacy Woyciechowski, Kristin Zelley, Kathleen D Valverde, Donna M McDonald-McGinn
Expanding Genetic Counselor Roles: A Model for Global Research Development. Genes 15 (7) (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, Terrence Blaine Crowley, Stephanie Asher, Amanda Back, Sarah M Baldino, Emma Bedoukian, Allison D Britt, Natalie Burrill, Cara Cacioppo, Dana Farengo Clark, Mary Egan Clark, Laura Conway, Laynie Dratch, Holly A Dubbs, Nicole M Engelhardt, Natalie Ginn, Christopher Gray, Tiff Hartman, Evan R Hathaway, Katherine L Helbig, Lily Hoffman-Andrews, Stefanie Kasperski, Beth A Keena, Kierstin N Keller, Katherine L Nathanson, Lauren Lulis, Laina Lusk, Daniel E McGinn, Rebecca Mueller, Rache A Paul, Lisa Pilchman, Jacquelyn Powers, Sarah E Raible, Sara Reichert, Alyssa L Ritter, Angela G Arnold, Sarah M Ruggiero, Erica Schindewolf, Katie Rose Sullivan, Shannon Terek, Bekah Wang, McKenzie Wells, Natalia Wisniewski, Renee Wright, Elisabeth McCarty Wood, Stacy Woyciechowski, Kristin Zelley, Kathleen D Valverde, Donna M McDonald-McGinn
Expanding Genetic Counselor Roles: A Model for Global Research Development. Genes 15 (7) (2024)
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson, Allison Elizabeth Ashley Koch, Hal S Meltzer, Joan Le, Kit Sing Au, Hope Northrup, Gyang Markus Bot, Valeria Capra, Richard H Finnell, Zoha Kibar, Philip J Lupo, Helio R Machado, Camila Araújo, Tony Magana, Ahmed I Marwan, Gia Melikishvili, Osvaldo M Mutchinick, Roger E Stevenson, Anna Yurrita, Maha S Zaki, Sara Mumtaz, José Ramón Medina-Bereciartu, Caroline M Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt, Mahmoud M Noureldeen, Aida Ms Salem, Yukitoshi Takahashi, Hormos Salimi-Dafsari, H Westley Phillips, Brian Hanak, Bülent Kara, Ayfer Sakarya Güneş, David D Gonda, Salman Kirmani, Tinatin Tkemaladze, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, Terrence Blaine Crowley, Stephanie Asher, Amanda Back, Sarah M Baldino, Emma Bedoukian, Allison D Britt, Natalie Burrill, Cara Cacioppo, Dana Farengo Clark, Mary Egan Clark, Laura Conway, Laynie Dratch, Holly A Dubbs, Nicole M Engelhardt, Natalie Ginn, Christopher Gray, Tiff Hartman, Evan R Hathaway, Katherine L Helbig, Lily Hoffman-Andrews, Stefanie Kasperski, Beth A Keena, Kierstin N Keller, Katherine L Nathanson, Lauren Lulis, Laina Lusk, Daniel E McGinn, Rebecca Mueller, Rache A Paul, Lisa Pilchman, Jacquelyn Powers, Sarah E Raible, Sara Reichert, Alyssa L Ritter, Angela G Arnold, Sarah M Ruggiero, Erica Schindewolf, Katie Rose Sullivan, Shannon Terek, Bekah Wang, McKenzie Wells, Natalia Wisniewski, Renee Wright, Elisabeth McCarty Wood, Stacy Woyciechowski, Kristin Zelley, Kathleen D Valverde, Donna M McDonald-McGinn
Expanding Genetic Counselor Roles: A Model for Global Research Development. Genes 15 (7) (2024)
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, Senne Meynants, Erika Souche, Ruben Cools, Tracy Heung, Koen Devriendt, Hilde Peeters, Donna M McDonald-McGinn, Ann Swillen, Jeroen Breckpot, Beverly S Emanuel, Hilde Van Esch, Anne Susan Bassett, Joris Robert Vermeesch
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome. bioRxiv : the preprint server for biology (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M McDonald-McGinn, T Blaine Crowley, Daniel E McGinn, Oanh T Tran, Daniella Miller, Jhih-Rong Lin, Elaine H Zackai, H Richard Johnston, Eva W C Chow, Jacob A S Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris Robert Vermeesch, Stephan Eliez, Maude Schneider, Marianne B M van den Bree, Michael J Owen, Wendy R Kates, Gabriela M Repetto, Vandana Shashi, Kelly Schoch, Carrie E Bearden, M Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C Murphy, Declan G M Murphy, Sixto García-Miñaúr, Luis Fernández, null null, Zhengdong D Zhang, Elizabeth Goldmuntz, Raquel E Gur, Beverly S Emanuel, Deyou Zheng, Christian R Marshall, Anne Susan Bassett, Tao Wang, Bernice E Morrow
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. NPJ genomic medicine 8 (1) (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Jente Verbesselt, Cynthia B Solot, Ellen Van Den Heuvel, Terrence Blaine Crowley, Victoria Giunta, Jeroen Breckpot, Donna M McDonald-McGinn, Inge Zink, Ann Swillen
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants. Genes 14 (3) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Jente Verbesselt, Cynthia B Solot, Ellen Van Den Heuvel, Terrence Blaine Crowley, Victoria Giunta, Jeroen Breckpot, Donna M McDonald-McGinn, Inge Zink, Ann Swillen
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants. Genes 14 (3) (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Jente Verbesselt, Cynthia B Solot, Ellen Van Den Heuvel, Terrence Blaine Crowley, Victoria Giunta, Jeroen Breckpot, Donna M McDonald-McGinn, Inge Zink, Ann Swillen
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants. Genes 14 (3) (2023)
Jhih-Rong Lin, Yingjie Zhao, M Reza Jabalameli, Nha Nguyen, Joydeep Mitra, null null, Ann Swillen, Jacob A S Vorstman, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Michael J Owen, Nigel M Williams, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur, Carrie E Bearden, Bernice E Morrow, Herbert M Lachman, Zhengdong D Zhang
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular psychiatry (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Daniel E McGinn, Terrence Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H Zackai, Beverly S Emanuel, Eva W C Chow, Bernice E Morrow, Ann Swillen, Anne Susan Bassett, Donna M McDonald-McGinn
Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes 13 (10) (2022)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Steven Pastor, Oanh Tran, Daniel E McGinn, Terrence Blaine Crowley, Elaine H Zackai, Donna M McDonald-McGinn, Beverly S Emanuel
A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome. Genes 13 (9) (2022)
Eli J Cornblath, Arun Mahadevan, Xiaosong He, Kosha Ruparel, David M Lydon-Staley, Tyler Maxwell Moore, Ruben C Gur, Elaine H Zackai, Beverly Emanuel, Donna M McDonald-McGinn, Daniel H Wolf, Theodore Daniel Satterthwaite, David R Roalf, Raquel E Gur, Danielle S Bassett
Altered functional brain dynamics in chromosome 22q11.2 deletion syndrome during facial affect processing. Molecular psychiatry (2021)
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, Tracy Heung, Aaron M Holleman, H Richard Johnston, Thomas Monfeuga, Donna M McDonald-McGinn, Raquel E Gur, Bernice E Morrow, Ann Swillen, Jacob A S Vorstman, Carrie E Bearden, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Stephen T Warren, Michael J Owen, Pankaj Chopra, David J Cutler, Richard Duncan, Alex V Kotlar, Jennifer G Mulle, Anna J Voss, Michael E Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih-Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I Salmons, Oanh Tran, Peter Holmans, Antonio F Pardinas, James T R Walters, Wolfram Demaerel, Erik Boot, Nancy J Butcher, Gregory A Costain, Chelsea Lowther, Rens Evers, Therese A M J van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koen Devriendt, Elfi Vergaelen, Annick Vogels, Terrence Blaine Crowley, Daniel E McGinn, Edward M Moss, Robert J Sharkus, Marta Unolt, Elaine H Zackai, Monica E Calkins, Robert S Gallagher, Ruben C Gur, Sunny X Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M Repetto, Elemi Breetvelt, Sasja N Duijff, Ania M Fiksinski, Hayley Moss, Maria Niarchou, Kieran C Murphy, Sarah E Prasad, Eileen M Daly, Maria Gudbrandsen, Clodagh M Murphy, Declan G M Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria C Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F Cubells, Opal Y Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori-Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider, Frédérique Sloan Béna, Kevin M Antshel, Wanda Fremont, Wendy R Kates, Raoul Belzeaux, Tiffany Busa, Nicole Philip, Linda E Campbell, Kathryn L McCabe, Stephen R Hooper, Kelly Schoch, Vandana Shashi, Tony J Simon, Flora Tassone, Celso Arango, David Fraguas, Sixto García-Miñaúr, Jaume Morey-Canyelles, Jordi Rosell, Damià H Suñer, Jasna Raventos-Simic, null null, Michael P Epstein, Nigel M Williams, Anne S Bassett
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular psychiatry 26 (8) (2020)
Robert William Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne Susan Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow, Donna M McDonald-McGinn, Ann Swillen, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Therese van Amelsvoort, Celso Arango, Marco Armando, Linda E Campbell, Joseph F Cubells, Stephan Eliez, Sixto Garcia-Minaur, Doron Gothelf, Wendy R Kates, Kieran C Murphy, Clodagh M Murphy, Declan G M Murphy, Nicole Philip, Gabriela M Repetto, Vandana Shashi, Tony J Simon, Damiàn Heine Suñer, Stefano Vicari, Stephen W Scherer, null null, Carrie E Bearden, Jacob A S Vorstman
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature medicine 26 (12) (2020)
Marta Unolt, Molka Kammoun, Sebastian Kwiatkowski, Gail E Graham, Terrence Blaine Crowley, Matthew S Hestand, Wolfram Demaerel, Maciej Geremek, Beverly S Emanuel, Elaine H Zackai, Joris R Vermeesch, Donna M McDonald-McGinn
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
E Verheij, L Elden, Terrence Blaine Crowley, Frank A Pameijer, Elaine H Zackai, Donna M McDonald-McGinn, Henricus G X M Thomeer
Anatomic Malformations of the Middle and Inner Ear in 22q11.2 Deletion Syndrome: Case Series and Literature Review. AJNR. American journal of neuroradiology 39 (5) (2018)
Jessica C Barry, Terrence Blaine Crowley, Soma Jyonouchi, Jennifer Heimall, Elaine H Zackai, Kathleen E Sullivan, Donna M McDonald-McGinn
Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency. Journal of clinical immunology 37 (5) (2017)

Donna M McDonald-McGinn.css-eqlu8i{font-size:small;padding-left:4px;} (Donna McDonald-McGinn, D M McDonald-McGinn)

Publication Activity (10 Years)

Top Topics

Top Venues

Donna M McDonald-McGinn (Donna McDonald-McGinn, D M McDonald-McGinn)